About: Robert Feil

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

researcher (ORCID 0000-0002-5671-5860)

Attributes	Values
rdf:type	Item
description	forskare (sv) 연구원 (ko) গবেষক (bn) 研究者 (ja) araştırmacı (tr) wetenschapper (nl) дослідник (uk) изилдөөчү (ky) 研究者 (zh) հետազոտող (hy) hulumtues (sq) researcher (ORCID 0000-0002-5671-5860) (en)
rdfs:label	Robert Feil (en) Robert Feil (es) Robert Feil (fr) Robert Feil (it) Robert Feil (nl) Robert Feil (sl) Robert Feil (ast)
skos:prefLabel	Robert Feil (en) Robert Feil (es) Robert Feil (fr) Robert Feil (it) Robert Feil (nl) Robert Feil (sl) Robert Feil (ast)
name	Robert Feil (en) Robert Feil (es) Robert Feil (fr) Robert Feil (it) Robert Feil (nl) Robert Feil (sl) Robert Feil (ast)
given name	wds:Q30380330-2228B8F0-C486-4696-A01A-877135C5D687
given name	Robert
instance of	wds:Q30380330-8102E9DF-F37B-469A-A95E-D7039A314664
instance of	Homo sapiens
occupation	wds:Q30380330-17888273-DEA6-4F21-B751-6E4DBCFF5D0C
sex or gender	wds:Q30380330-15F91B4A-56C1-4A53-9CC4-F8B68889216A
VIAF ID	wds:Q30380330-2EF7FC94-5249-423A-97E2-A0F7B2771C0A
IdRef ID	wds:Q30380330-EB1A17D0-96A3-4FA3-8463-6F765C895FF0
date of birth	wds:Q30380330-971393E4-2019-4442-8661-42114D6EE26B
family name	wds:Q30380330-989A3FB0-31E6-4DE3-9268-2B9ED919AABF
VIAF ID	http://viaf.org/viaf/172447036
IdRef ID	http://www.idref.fr/097720909/id
occupation	researcher
sex or gender	male
VIAF ID	172447036
IdRef ID	097720909
date of birth	1961-01-01 00:00:00Z (xsd:dateTime)
family name	Feil
Springer Nature person ID	wds:Q30380330-9B3F6A79-AB08-41E7-9465-2FA105A72625
ORCID iD	wds:Q30380330-3B21246D-CF4A-4C4B-9657-B5C2177CADC4
Dimensions author ID	wds:Q30380330-C9C1AF52-0AD1-4A87-BA87-92D89925692B
ORCID iD	https://orcid.org/0000-0002-5671-5860
Springer Nature person ID	011551375620.15
ORCID iD	0000-0002-5671-5860
Dimensions author ID	011551375620.15
ResearcherID	wds:Q30380330-30E7C9EB-D791-4BB0-9149-656EF7556129
Publons author ID	wds:Q30380330-08601e6a-f26b-41c2-ba92-bc62d47269f2
ResearcherID	D-2087-2013
Publons author ID	2659251
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q30380330
is author of	Epigenetic asymmetry in the zygote and mammalian development Epigenetic regulation of mammalian genomic imprinting Impairment of LTD and cerebellar learning by Purkinje cell-specific ablation of cGMP-dependent protein kinase I cGMP-dependent protein kinase II modulates mPer1 and mPer2 gene induction and influences phase shifts of the circadian clock Global hypomethylation of the genome in XX embryonic stem cells. Epigenetics and the environment: emerging patterns and implications Culture of preimplantation embryos and its long-term effects on gene expression and phenotype. Identification of the imprinted KLF14 transcription factor undergoing human-specific accelerated evolution A bivalent chromatin structure marks key developmental genes in embryonic stem cells Putative X-linked adrenoleukodystrophy gene shares unexpected homology with ABC transporters IRAG is essential for relaxation of receptor-triggered smooth muscle contraction by cGMP kinase Histone methylation is mechanistically linked to DNA methylation at imprinting control regions in mammals Human imprinted retrogenes exhibit non-canonical imprint chromatin signatures and reside in non-imprinted host genes The Air noncoding RNA epigenetically silences transcription by targeting G9a to chromatin DNA methylation is linked to deacetylation of histone H3, but not H4, on the imprinted genes Snrpn and U2af1-rs1. LKB1 signaling in mesenchymal cells required for suppression of gastrointestinal polyposis Synergic reprogramming of mammalian cells by combined exposure to mitotic Xenopus egg extracts and transcription factors Allelic inactivation of the pseudoautosomal gene SYBL1 is controlled by epigenetic mechanisms common to the X and Y chromosomes Conservation of IGF2-H19 and IGF2R imprinting in sheep: effects of somatic cell nuclear transfer. Small regulatory RNAs controlled by genomic imprinting and their contribution to human disease Environmental and nutritional effects on the epigenetic regulation of genes Allele-specific histone lysine methylation marks regulatory regions at imprinted mouse genes Convergent evolution of genomic imprinting in plants and mammals. Differential histone modifications mark mouse imprinting control regions during spermatogenesis. Genomic imprinting in ruminants: allele-specific gene expression in parthenogenetic sheep. A 195-kb cosmid walk encompassing the human Xq28 color vision pigment genes An essential role of Cav1.2 L-type calcium channel for urinary bladder function p8-deficient fibroblasts grow more rapidly and are more resistant to adriamycin-induced apoptosis Impaired insulin secretion and glucose tolerance in beta cell-selective Ca(v)1.2 Ca2+ channel null mice MEDEA takes control of its own imprinting Elevated blood pressure linked to primary hyperaldosteronism and impaired vasodilation in BK channel-deficient mice Parental chromosome-specific chromatin conformation in the imprinted U2af1-rs1 gene in the mouse. Chromatin mechanisms in the developmental control of imprinted gene expression Genome-wide DNA demethylation in mammals Multiple imprinted sense and antisense transcripts, differential methylation and tandem repeats in a putative imprinting control region upstream of mouse Igf2. The hyperpolarization-activated channel HCN4 is required for the generation of pacemaker action potentials in the embryonic heart

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